Mechanistische Analysen zu Krankheits-korrelierten SNPs in ...

7 Literaturverzeichnis
[99] DUAN, R. ; PAK, C. ; JIN, P.: Single nucleotide polymorphism associated with mature miR-125a
alters the processing of pri-miRNA. In: Hum Mol Genet 16 (2007), S. 1124–31
[100] TIAN, T. ; SHU, Y. ; CHEN, J. ; HU, Z. ; XU, L. ; JIN, G. ; LIANG, J. ; LIU, P. ; ZHOU, X. ; MIAO, R.
; MA, H. ; CHEN, Y. ; SHEN, H.: A functional genetic variant in microRNA-196a2 is associated
with increased susceptibility of lung cancer in Chinese. In: Cancer Epidemiol Biomarkers Prev
18 (2009), S. 1183–7
[101] XU, J. ; HU, Z. ; XU, Z. ; GU, H. ; YI, L. ; CAO, H. ; CHEN, J. ; TIAN, T. ; LIANG, J. ; LIN, Y. ; QIU,
W. ; MA, H. ; SHEN, H. ; CHEN, Y.: Functional variant in microRNA-196a2 contributes to the
susceptibility of congenital heart disease in a Chinese population. In: Hum Mutat 30 (2009), S.
1231–1236
[102] HU, Z. ; CHEN, J. ; TIAN, T. ; ZHOU, X. ; GU, H. ; XU, L. ; ZENG, Y. ; MIAO, R. ; JIN, G. ; MA, H.
; CHEN, Y. ; SHEN, H.: Genetic variants of miRNA sequences and non-small cell lung cancer
survival. In: J Clin Invest 118 (2008), S. 2600–8
[103] LEE, H. C. ; YANG, C. W. ; CHEN, C. Y. ; AU, L. C.: Single point mutation of microRNA may cause
butterfly effect on alteration of global gene expression. In: Biochem Biophys Res Commun
(2010)
[104] GLINSKY, G. V.: An SNP-guided microRNA map of fifteen common human disorders identifies a
consensus disease phenocode aiming at principal components of the nuclear import pathway.
In: Cell Cycle 7 (2008), S. 2570–83
[105] ABELSON, J. F. ; KWAN, K. Y. ; O’ROAK, B. J. ; BAEK, D. Y. ; STILLMAN, A. A. ; MORGAN, T. M. ;
MATHEWS, C. A. ; PAULS, D. L. ; RASIN, M.-R. ; GUNEL, M. ; DAVIS, N. R. ; ERCAN-SENCICEK,
A. G. ; GUEZ, D. H. ; SPERTUS, J. A. ; LECKMAN, J. F. ; DURE 4TH, L. S. ; KURLAN, R. ;
SINGER, H. S. ; GILBERT, D. L. ; FARHI, A. ; LOUVI, A. ; LIFTON, R. P. ; SESTAN, N. ; STATE,
M. W.: Sequence variants in SLITRK1 are associated with Tourette’s syndrome. In: Science
310 (2005), S. 317–320
[106] WANG, G. ; VAN DER WALT, J. M. ; MAYHEW, G. ; LI, Y.-J. ; ZÜCHNER, S. ; SCOTT, W. K. ;
MARTIN, E. R. ; VANCE, J. M.: Variation in the miRNA-433 binding site of FGF20 confers risk
for Parkinson disease by overexpression of alpha-synuclein. In: Am J Hum Genet 82 (2008),
S. 283–289
[107] CLOP, A. ; MARCQ, F. ; TAKEDA, H. ; PIROTTIN, D. ; TORDOIR, X. ; BIBÉ, B. ; BOUIX, J. ;
CAIMENT, F. ; ELSEN, J. ; EYCHENNE, F. ; LARZUL, C. ; LAVILLE, E. ; MEISH, F. ; MILENKOVIC,
D. ; TOBIN, J. ; CHARLIER, C. ; GEORGES, M.: A mutation creating a potential illegitimate
microRNA target site in the myostatin gene affects muscularity in sheep. In: Nat Genet 38
(2006), S. 813–818
[108] HU, Z. ; BRUNO, A. E.: The Influence of 3’UTRs on MicroRNA Function Inferred from Human
SNP Data. In: Comp Funct Genomics 2011 (2011), S. 910769
[109] YE, Y. ; WANG, K. K. ; GU, J. ; YANG, H. ; LIN, J. ; AJANI, J. A. ; WU, X.: Genetic variations
in microRNA-related genes are novel susceptibility loci for esophageal cancer risk. In: Cancer
Prev Res (Phila) 1 (2008), S. 460–9
[110] LIN, J. ; HORIKAWA, Y. ; TAMBOLI, P. ; CLAGUE, J. ; WOOD, C. G. ; WU, X.: Genetic variations
in microRNA-related genes are associated with survival and recurrence in patients with renal
cell carcinoma. In: Carcinogenesis 31 (2010), S. 1805–1812
[111] KIM, J.-S. ; CHOI, Y. Y. ; JIN, G. ; KANG, H.-G. ; CHOI, J.-E. ; JEON, H.-S. ; LEE, W.-K. ; KIM,
D.-S. ; KIM, C. H. ; KIM, Y. J. ; SON, J.-W. ; JUNG, T. H. ; PARK, J. Y.: Association of a common
AGO1 variant with lung cancer risk: a two-stage case-control study. In: Mol Carcinog 49 (2010),
S. 913–921
[112] LARSSON, E. ; SANDER, C. ; MARKS, D.: mRNA turnover rate limits siRNA and microRNA
159